Oncology Clinical Physician

The Oncology Clinical Physician plays a crucial role in overseeing medical responsibilities throughout clinical trials within the Clinical Development & Operations team. This position is suited for a qualified and experienced physician who will provide medical guidance from the trial's initiation to the final reporting of results. As a vital member of both the Trial Team and Evidence Network Team, this physician will contribute valuable medical insights across all phases of the clinical trial process. Trial Start-Up Collaborate with clinical leaders and team members to guarantee the highest quality standards in the medical content of Clinical Trial Protocols (CTPs) and update them based on medical insights. Identify critical clinical data and processes to support trial risk management and the Integrated Quality and Risk Management Plan (IQRMP). Help create a robust Clinical Quality Monitoring Plan (CQMP) focused on ensuring medical quality and risk mitigation. Provide oversight on determining significant protocol deviations and aid in the clinical evaluation of these deviations. Ensure timely preparation of all core trial documents, ensuring they meet required medical standards. Contribute medical input into Data Management documents to guarantee accurate electronic data capture and consistency. Be responsible for the medical content of patient-facing documents, communication plans, and statistical analysis plans. Review Patient Narratives and assist in planning and evaluating Clinical Trial Reports. Draft responses to inquiries from regulatory authorities and Ethics Committees/IRBs as necessary. Offer insights during study and site feasibility assessments, as well as patient recruitment strategies. Facilitate medical training sessions for trial investigators and sponsor staff as required. Trial Conduct Carry out ongoing medical reviews, thoroughly documenting findings and resolutions. Execute clinical quality monitoring following the CQMP, proactively addressing any arising risks and issues. Engage in proactive medical oversight using contemporary data management technologies and tools. Work collaboratively with team members to communicate and resolve any clinical quality issues effectively. Address inconsistencies in medical data and challenges pertaining to study protocol execution promptly. Respond to medical inquiries from Investigators and relevant stakeholders, maintaining a trial FAQ log. Build a network with subject matter experts to enhance site engagement. Support meetings with committees such as Endpoint Adjudication or Data Safety Monitoring Boards by providing medical updates and addressing questions. Contribute to the development of trial newsletters and scientific publications if applicable. Leadership Oversee medical activities across multiple clinical trials. Plan and analyze clinical programs collaboratively in a cross-functional environment. Be accountable for medical assessments and quality decisions throughout trial processes. Compliance with Standards Adhere to training requirements and company policies. Accurately complete timesheets and timely submit expense reports. Maintain an updated CV that complies with regulatory guidelines and standards. Skills: Proficient in Microsoft Office Suite (Word, PowerPoint, Excel, Outlook). Fluent in English; knowledge of additional local languages is preferred. Strong interpersonal, analytical, and presentation skills. Able to work effectively in a collaborative international environment. Skilled in leveraging digital technology for innovative problem-solving. Experience: A minimum of 4 years of clinical experience as a physician (MD), ideally specializing in internal medicine or general practice. Experience in the pharmaceutical industry or a CRO in relevant medical roles, with a strong understanding of ICH-GCP regulations. Familiarity with data visualization and IT systems. Parexel is an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Created: 2026-03-04